Alagille syndrome associated conditions: Difference between revisions
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{{Alagille syndrome}} | |||
{{CMG}} | |||
==Overview== | |||
'''Alagille syndrome''' is a multisystem [[genetic disorder]] that affects the [[liver]], [[heart]], [[eyes]],[[face]], [[skeleton]], [[kidneys]] and [[vascular system]]. | |||
==Associated Conditions== | |||
Alagille syndrome can be associated with [[congenital heart disease]], particularly [[Tetralogy of Fallot]]. The[[kidney]]s and [[central nervous system]] may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome. | Alagille syndrome can be associated with [[congenital heart disease]], particularly [[Tetralogy of Fallot]]. The[[kidney]]s and [[central nervous system]] may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome. | ||
==References== | |||
{{reflist|2}} | |||
[[Category:Pediatrics]] | |||
[[Category:Gastroenterology]] | |||
[[Category:Genetic disorders]] | |||
[[Category:Rare diseases]] | |||
[[Category:Hepatology]] | |||
[[Category:Mature chapter]] | |||
{{WH}} | |||
{{WS}} |
Revision as of 17:33, 23 September 2011
Alagille syndrome Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Alagille syndrome is a multisystem genetic disorder that affects the liver, heart, eyes,face, skeleton, kidneys and vascular system.
Associated Conditions
Alagille syndrome can be associated with congenital heart disease, particularly Tetralogy of Fallot. Thekidneys and central nervous system may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome.